Zhang, Z., Liu, X., Liu, T. et al. Polypeptide from Chlamys farreri inhibits UVB-induced apoptosis of HaCaT cells via iNOS/NO and HSP90., Chin. J. Ocean. Limnol. 27, 594–599 (2009). https://doi.org/10.1007/s00343-009-9171-6
DOI:
Zhang, Z., Liu, X., Liu, T. et al. Polypeptide from Chlamys farreri inhibits UVB-induced apoptosis of HaCaT cells via iNOS/NO and HSP90., Chin. J. Ocean. Limnol. 27, 594–599 (2009). https://doi.org/10.1007/s00343-009-9171-6DOI:
Polypeptide from Chlamys farreri inhibits UVB-induced apoptosis of HaCaT cells via iNOS/NO and HSP90
摘要
Abstract
Polypeptide from Chlamys farreri (PCF) is a novel marine bioactive product that was isolated from the gonochoric Chinese scallop Chlamys farreri
and was found to be an effective antioxidant in our recent studies. In this study
we investigated the effect of PCF on ultraviolet B (UVB)-induced apoptosis of HaCaT cells and the intracellular signaling pathways involved. Pretreatment with the inducible nitric oxide synthase (iNOS) inhibitor S-methylisothiourea sulfate inhibited UVB-induced apoptosis
indicating that iNOS and NO play important roles in apoptosis. On the other hand
the inhibition of UVB-induced apoptosis in the immortalized keratinocyte (HaCaT) cells by PCF was estimated using a DNA ladder. PCF treatment inhibited UVB-induced iNOS activation
as determined by RT-PCR
NO production
as determined by ESR
and up-regulated heat shock protein (HSP) 90 activation
as determined by Western blotting. Our results indicate that iNOS and NO are involved in UVB-induced apoptosis of HaCaT cells and the protective effect of PCF against UVB irradiation is exerted by suppressing the expression of iNOS
followed by inhibition of NO release and enhanced activation of HSP90.
关键词
Keywords
references
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